Canonical Allele Identifier: CA2579600557
Gene: WAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683757T>A , CM000685.2:g.48683757T>A GRCh38
NC_000023.10:g.48542146T>A , CM000685.1:g.48542146T>A GRCh37
NC_000023.9:g.48427090T>A NCBI36
NG_007877.1:g.4961T>A , LRG_125:g.4961T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-63T>A ENSP00000513844.1:n.-34-63T>A
ENST00000450772.5:c.-34-63T>A ENSP00000410537.1:n.-34-63T>A
XM_017029786.1:c.-97T>A XP_016885275.1:n.-97T>A
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